SPOR Status Update, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 22 January 2025, 10:00 (CET) to 22 January 2025, 12:30 (CET)

Submitted by Anonymous (not verified) on 21 January 2025 - 15:10

SPOR Status Update, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 22 January 2025, 10:00 (CET) to 22 January 2025, 12:30 (CET)

Questions and answers to stakeholders on the implications of Regulation (EU) 2023/1182 for centrally authorised medicinal products for human use

Submitted by Anonymous (not verified) on 21 January 2025 - 12:53

Questions and answers to stakeholders on the implications of Regulation (EU) 2023/1182 for centrally authorised medicinal products for human use

Human medicines European public assessment report (EPAR): Posaconazole AHCL, posaconazole, Date of authorisation: 25/07/2019, Revision: 10, Status: Authorised

Submitted by Anonymous (not verified) on 21 January 2025 - 8:56

Human medicines European public assessment report (EPAR): Posaconazole AHCL, posaconazole, Date of authorisation: 25/07/2019, Revision: 10, Status: Authorised

Human medicines European public assessment report (EPAR): Potactasol, topotecan, Date of authorisation: 06/01/2011, Revision: 12, Status: Authorised

Submitted by Anonymous (not verified) on 20 January 2025 - 16:20

Human medicines European public assessment report (EPAR): Potactasol, topotecan, Date of authorisation: 06/01/2011, Revision: 12, Status: Authorised

Human medicines European public assessment report (EPAR): Levitra, vardenafil, Date of authorisation: 06/03/2003, Revision: 34, Status: Authorised

Submitted by Anonymous (not verified) on 20 January 2025 - 16:16

Human medicines European public assessment report (EPAR): Levitra, vardenafil, Date of authorisation: 06/03/2003, Revision: 34, Status: Authorised

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